(Q28267610)

12

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author name string

B Devlin

1

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E H Cook

2

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H Coon

3

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G Dawson

4

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E L Grigorenko

5

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W McMahon

6

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N Minshew

7

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D Pauls

8

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M Smith

9

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M A Spence

10

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P M Rodier

11

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G D Schellenberg

Acute tryptophan depletion in autistic disorder: a controlled case study

13

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language of work or name

English

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publication date

December 2005

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published in

Molecular Psychiatry

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volume

10

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issue

12

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page(s)

1110-6

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cites work

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Developmental changes in brain serotonin synthesis capacity in autistic and nonautistic children

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

A double-blind, placebo-controlled study of fluvoxamine in adults with autistic disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Platelet serotonin studies in hyperserotonemic relatives of children with autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Evidence of linkage between the serotonin transporter and autistic disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Serotonin transporter (5-HTT) gene variants associated with autism?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

A genomic screen of autism: evidence for a multilocus etiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

A genomewide screen of 345 families for autism-susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Evolutionary-based association analysis using haplotype data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Allegro, a new computer program for multipoint linkage analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Power calculations for a general class of family-based association tests: dichotomous traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

The TDT reveals linkage and linkage disequilibrium in a rare disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Evidence for sex-specific risk alleles in autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Serotonin transporter gene promoter variants do not explain the hyperserotoninemia in autistic children

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Variants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Autism, affective disorders, and social phobia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Autism, affective and other psychiatric disorders: patterns of familial aggregation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Personality traits of the relatives of autistic probands.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Meta-analysis of the association between a serotonin transporter promoter polymorphism (5-HTTLPR) and anxiety-related personality traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Evidence for linkage disequilibrium between serotonin transporter protein gene (SLC6A4) and obsessive compulsive disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Role of the serotonin transporter gene in the behavioral expression of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Serotonin transporter gene and autism: a haplotype analysis in an Irish autistic population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Evidence for an association with the serotonin transporter promoter region polymorphism and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

Allelic Variation of Human Serotonin Transporter Gene Expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

The serotonin system in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

2-year-old boy who has been diagnosed with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

inferred from DOI database lookup

7 January 2021

based on heuristic

On a general class of conditional tests for family-based association studies in genetics: the asymptotic distribution, the conditional power, and optimality considerations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724

inferred from DOI database lookup

7 January 2021

based on heuristic

Organization of the human serotonin transporter gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001724